Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs11953630 5 158418394 intergenic variant C/A;T snv 6
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs419076
MECOM
3 169383098 intron variant T/A;C snv 6
rs4373814 10 18131043 intergenic variant G/C;T snv 5
rs448378
MECOM
1.000 0.040 3 169383111 intron variant G/A;C snv 5
rs2392929 7 106773623 upstream gene variant T/A;C;G snv 4
rs2932538
MOV10
1 112673921 intron variant A/C;G snv 4
rs4759319
HOXC4 ; HOXC6 ; HOXC5
12 54030947 intron variant G/C;T snv 4
rs7577262 2 233910224 intergenic variant G/A;T snv 4
rs13280442 8 11610048 intergenic variant C/A;G snv 3
rs2681485
ATP2B1
12 89631845 intron variant G/A;T snv 3
rs4841465
XKR6
8 10962344 intron variant C/G;T snv 3
rs588321
LSP1
11 1875727 intron variant G/C;T snv 3
rs11693319
CCDC141
2 178873542 3 prime UTR variant C/G;T snv 2
rs4841294
MSRA
8 10247558 intron variant C/A;T snv 2
rs576603 11 1892909 upstream gene variant C/A;G;T snv 2
rs7658266
ARSJ
4 113942550 intron variant T/A;C snv 2